Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+

The reaction of [Ru(bpy)2(NO)Cl]2+ with 2,2,2-trifluoroethylamine produced [Ru(bpy)2(NO)Cl]+ by electron transfer and a number of organic compounds formed via nucleophilic substitution of the intermediate 2,2,2-trifluoroethyldiazonium ion (free or coordinated). Density functional theory computed res...

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Autores principales: Di Salvo, Florencia, Crespo, Alejandro, Estrin, Dario Ariel, Doctorovich, Fabio Ariel
Publicado: 2002
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v58_n21_p4237_DiSalvo
http://hdl.handle.net/20.500.12110/paper_00404020_v58_n21_p4237_DiSalvo
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spelling paper:paper_00404020_v58_n21_p4237_DiSalvo2023-06-08T15:04:15Z Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+ Di Salvo, Florencia Crespo, Alejandro Estrin, Dario Ariel Doctorovich, Fabio Ariel 2,2,2-trifluoroethylamine Complex Density functional theory Electron transfer n-butylamine Nitrosyl Ruthenium 2,2,2 trifluoroethylamine butylamine ethylamine ruthenium complex unclassified drug article calculation chemical reaction complex formation electron transport molecular stability priority journal reaction analysis solvation theory The reaction of [Ru(bpy)2(NO)Cl]2+ with 2,2,2-trifluoroethylamine produced [Ru(bpy)2(NO)Cl]+ by electron transfer and a number of organic compounds formed via nucleophilic substitution of the intermediate 2,2,2-trifluoroethyldiazonium ion (free or coordinated). Density functional theory computed results suggest that stabilization of the trifluoroethyldiazonium ion by complexation is much larger than the one corresponding to the butyl ion, in agreement with the fact that no rearrangement products derived from CF3CH2+ were observed. © 2002 Elsevier Science Ltd. All rights reserved. Fil:Di Salvo, F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Crespo, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Estrin, D.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Doctorovich, F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2002 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v58_n21_p4237_DiSalvo http://hdl.handle.net/20.500.12110/paper_00404020_v58_n21_p4237_DiSalvo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 2,2,2-trifluoroethylamine
Complex
Density functional theory
Electron transfer
n-butylamine
Nitrosyl
Ruthenium
2,2,2 trifluoroethylamine
butylamine
ethylamine
ruthenium complex
unclassified drug
article
calculation
chemical reaction
complex formation
electron transport
molecular stability
priority journal
reaction analysis
solvation
theory
spellingShingle 2,2,2-trifluoroethylamine
Complex
Density functional theory
Electron transfer
n-butylamine
Nitrosyl
Ruthenium
2,2,2 trifluoroethylamine
butylamine
ethylamine
ruthenium complex
unclassified drug
article
calculation
chemical reaction
complex formation
electron transport
molecular stability
priority journal
reaction analysis
solvation
theory
Di Salvo, Florencia
Crespo, Alejandro
Estrin, Dario Ariel
Doctorovich, Fabio Ariel
Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+
topic_facet 2,2,2-trifluoroethylamine
Complex
Density functional theory
Electron transfer
n-butylamine
Nitrosyl
Ruthenium
2,2,2 trifluoroethylamine
butylamine
ethylamine
ruthenium complex
unclassified drug
article
calculation
chemical reaction
complex formation
electron transport
molecular stability
priority journal
reaction analysis
solvation
theory
description The reaction of [Ru(bpy)2(NO)Cl]2+ with 2,2,2-trifluoroethylamine produced [Ru(bpy)2(NO)Cl]+ by electron transfer and a number of organic compounds formed via nucleophilic substitution of the intermediate 2,2,2-trifluoroethyldiazonium ion (free or coordinated). Density functional theory computed results suggest that stabilization of the trifluoroethyldiazonium ion by complexation is much larger than the one corresponding to the butyl ion, in agreement with the fact that no rearrangement products derived from CF3CH2+ were observed. © 2002 Elsevier Science Ltd. All rights reserved.
author Di Salvo, Florencia
Crespo, Alejandro
Estrin, Dario Ariel
Doctorovich, Fabio Ariel
author_facet Di Salvo, Florencia
Crespo, Alejandro
Estrin, Dario Ariel
Doctorovich, Fabio Ariel
author_sort Di Salvo, Florencia
title Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+
title_short Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+
title_full Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+
title_fullStr Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+
title_full_unstemmed Reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [Ru(bpy)2(NO)Cl]2+
title_sort reaction pathways of 2,2,2-trifluoroethylamine and n-butylamine with [ru(bpy)2(no)cl]2+
publishDate 2002
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404020_v58_n21_p4237_DiSalvo
http://hdl.handle.net/20.500.12110/paper_00404020_v58_n21_p4237_DiSalvo
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AT estrindarioariel reactionpathwaysof222trifluoroethylamineandnbutylaminewithrubpy2nocl2
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